Evidence map›Paper›PMID 16720700›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Plant-derived anti-Lewis Y mAb exhibits biological activities for efficient immunotherapy against human cancer cells.

Robert Brodzik, Magdalena Glogowska, Katarzyna Bandurska, Monika Okulicz, Deepali Deka, Kisung Ko, Joke van der Linden, Jeanette H W Leusen, Natalia Pogrebnyak, Maxim Golovkin and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
7.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 89 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Expression of recombinant vaccines and antibodies in plants.Monoclonal antibodies in immunodiagnosis and immunotherapy · 2014
    Review
  14. Article
  15. Article
  16. Evolution of plant-made pharmaceuticals.International journal of molecular sciences · 2011
    Review
  17. Article
  18. Identification of mRNA splicing factors as the endothelial receptor for carbohydrate-dependent lung colonization of cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  19. Article
  20. Plant-derived EpCAM antigen induces protective anti-cancer response.Cancer immunology, immunotherapy : CII · 2008
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Robert BrodzikBiotechnology Foundation Laboratories, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Magdalena Glogowska
Katarzyna Bandurska
Monika Okulicz
Deepali Deka
Kisung Ko
Joke van der Linden
Jeanette H W Leusen
Natalia Pogrebnyak
Maxim Golovkin
Zenon Steplewski
Hilary Koprowski
Thomas Jefferson University · USUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although current demands for therapeutic mAbs are growing quickly, production methods to date, including in vitro mammalian tissue culture and transgenic animals, provide only limited quantities at high cost. Several tumor-associated antigens in tumor cells have been identified as targets for therapeutic mAbs. Here we describe the production of mAb BR55-2 (IgG2a) in transgenic plants that recognizes the nonprotein tumor-associated antigen Lewis Y oligosaccharide overexpressed in human carcinomas, particularly breast and colorectal cancers. Heavy and light chains of mAb BR55-2 were expressed separately and assembled in plant cells of low-alkaloid tobacco transgenic plants (Nicotiana tabacum cv. LAMD609). Expression levels of plant-derived mAb (mAbP) were high (30 mg/kg of fresh leaves) in T1 generation plants. Like the mammalian-derived mAbM, the plant mAbP bound specifically to both SK-BR3 breast cancer cells and SW948 colorectal cancer cells. The Fc domain of both mAbP and mAbM showed the similar binding to FcgammaRI receptor (CD64). Comparable levels of cytotoxicity against SK-BR3 cells were also shown for both mAbs in antibody-dependent cell-mediated cytotoxicity assay. Furthermore, plant-derived BR55-2 efficiently inhibited SW948 tumor growth xenografted in nude mice. Altogether, these findings suggest that mAbP originating from low-alkaloid tobacco exhibit biological activities suitable for efficient immunotherapy.

Indexed as

Immunotherapy3T3 CellsAnimalsAntibodies, MonoclonalAntibody-Dependent Cell CytotoxicityAntibody SpecificityFlow CytometryGene ExpressionHumansImmunoglobulin Fc FragmentsLewis Blood Group AntigensMiceMice, Inbred BALB CMice, NudeNeoplasmsNicotianaAntibodies, MonoclonalImmunoglobulin Fc FragmentsLewis Blood Group AntigensLewis Y antigenPlantibodiesReceptors, IgG

Identifiers

PMID16720700
PMCPMC1482659
OpenAlexW2092366883

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.